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Journal Abstract Search

191 related items for PubMed ID: 33309813

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  • 2. Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responses.
    Kutsuma T, Katagiri S, Hayashi T, Yoshitake K, Iejima D, Gekka T, Kohzaki K, Mizobuchi K, Baba Y, Terauchi R, Matsuura T, Ueno S, Iwata T, Nakano T.
    Doc Ophthalmol; 2019 Jun; 138(3):229-239. PubMed ID: 30877594
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  • 3. Clinical course of two siblings with potassium voltage-gated channel modifier subfamily V member 2 (KCNV2)-associated retinopathy.
    Sato T, Kuniyoshi K, Hayashi T, Nishiwaki H, Mizobuchi K, Kusaka S.
    Doc Ophthalmol; 2024 Jun; 148(3):173-182. PubMed ID: 38630375
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  • 4. KCNV2-associated retinopathy: genotype-phenotype correlations - KCNV2 study group report 3.
    de Guimaraes TAC, Georgiou M, Robson AG, Fujinami K, Vincent A, Nasser F, Khateb S, Mahroo OA, Pontikos N, Vargas ME, Thiadens AAHJ, Carvalho ER, Nguyen XT, Arno G, Fujinami-Yokokawa Y, Liu X, Tsunoda K, Hayashi T, Jiménez-Rolando B, Martin-Merida MI, Avila-Fernandez A, Salas EC, Garcia-Sandoval B, Ayuso C, Sharon D, Kohl S, Huckfeldt RM, Banin E, Pennesi ME, Khan AO, Wissinger B, Webster AR, Heon E, Boon CJF, Zrenner E, Michaelides M.
    Br J Ophthalmol; 2024 Jul 23; 108(8):1137-1144. PubMed ID: 37852740
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  • 8. Fundus autofluorescence, optical coherence tomography and electroretinography abnormalities in a patient with digoxin retinopathy that resemble those in KCNV2-associated retinopathy.
    Nagae Y, Kuniyoshi K, Ishibashi M, Tanabe F, Matsumoto C, Kusaka S.
    Doc Ophthalmol; 2023 Oct 23; 147(2):131-137. PubMed ID: 37460904
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  • 9. MERTK retinopathy: biomarkers assessing vision loss.
    Sakti DH, Cornish EE, Mustafic N, Zaheer A, Retsas S, Rajagopalan S, Chung CW, Ewans L, McCluskey P, Nash BM, Jamieson RV, Grigg JR.
    Ophthalmic Genet; 2021 Dec 23; 42(6):706-716. PubMed ID: 34289798
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  • 10. Long-term follow-up of a Chinese patient with KCNV2-retinopathy.
    Lie H, Wang G, Liu X, Meng X, Long Y, Ren J, Yang L, Fujinami-Yokokawa Y, Kurihara T, Tsubota K, Fujinami K, Li S.
    Ophthalmic Genet; 2021 Apr 23; 42(2):144-149. PubMed ID: 33372566
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  • 12. Enhanced S-Cone Syndrome: Spectrum of Clinical, Imaging, Electrophysiologic, and Genetic Findings in a Retrospective Case Series of 56 Patients.
    de Carvalho ER, Robson AG, Arno G, Boon CJF, Webster AA, Michaelides M.
    Ophthalmol Retina; 2021 Feb 23; 5(2):195-214. PubMed ID: 32679203
    [Abstract] [Full Text] [Related]

  • 13. Visual Function in Carriers of X-Linked Retinitis Pigmentosa.
    Comander J, Weigel-DiFranco C, Sandberg MA, Berson EL.
    Ophthalmology; 2015 Sep 23; 122(9):1899-906. PubMed ID: 26143542
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  • 14. Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
    Sandberg MA, Rosner B, Weigel-DiFranco C, Dryja TP, Berson EL.
    Invest Ophthalmol Vis Sci; 2007 Mar 23; 48(3):1298-304. PubMed ID: 17325176
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  • 15. Psychophysically determined full-field stimulus thresholds (FST) in retinitis pigmentosa: relationships with electroretinography and visual field outcomes.
    Messias K, Jägle H, Saran R, Ruppert AD, Siqueira R, Jorge R, Messias A.
    Doc Ophthalmol; 2013 Oct 23; 127(2):123-9. PubMed ID: 23733195
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  • 17. Natural history and biomarkers of KCNV2-associated retinopathy.
    Sakti DH, Cornish EE, Ali H, Retsas S, Raza M, Saakova N, Carvalho LS, Nash BM, Jamieson RV, Grigg JR.
    Clin Exp Ophthalmol; 2024 Jul 23; 52(5):528-544. PubMed ID: 38443311
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  • 18. Retinal and visual function in infants with non-accidental trauma and retinal hemorrhages.
    Kelly JP, Feldman K, Wright J, Ganti S, Metz JB, Weiss A.
    Doc Ophthalmol; 2020 Oct 23; 141(2):111-126. PubMed ID: 32052259
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  • 19. Analysis of retinal structure and function in cone dystrophy with supernormal rod response.
    Abdelkader E, Yasir ZH, Khan AM, Raddadi O, Khandekar R, Alateeq N, Nowilaty S, AlShahrani N, Schatz P.
    Doc Ophthalmol; 2020 Aug 23; 141(1):23-32. PubMed ID: 31960170
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